chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1172228099172228100CT27GENICpossibly homozygous596159735
1172228157172228158AG22GENIChomozygous596159736
1172229335172229336TG22GENICheterozygous596159737
1172229594172229595GGACC15GENIChomozygous726375023
1172230036172230037CT10GENIChomozygous596159738
1172230042172230043C-9GENIChomozygous726375024
1172230454172230455TC20GENIChomozygous596159739
1172230961172230962AG9GENIChomozygous596159740
1172230972172230973GA3GENIChomozygous596159741
1172231004172231005C-14GENIChomozygous726375025
1172231339172231340GA13GENICpossibly homozygous596159742
1172231528172231529A-6GENIChomozygous726375026
1172231556172231557CCT2GENICheterozygous726375027
1172233075172233076AC1GENIChomozygous598194622
1172233269172233270TC31GENICpossibly homozygous596159743
1172233416172233417CT33GENICpossibly homozygous596159744
1172234597172234598TC12GENIChomozygous596159745
1172234600172234601AG13GENIChomozygous596159746
1172234711172234712AAT4GENIChomozygous726375029
1172234931172234941ACAGACAGAC----------15GENICpossibly homozygous726375030
1172235064172235065CT16GENIChomozygous596159747
1172235892172235893TC28GENICpossibly homozygous596159748
1172237383172237384AG18GENICheterozygous596159749
1172237548172237549TTGTGTGTGTGA2GENIChomozygous726375031
1172237593172237594AG14GENIChomozygous596159750
1172237694172237695CT3GENIChomozygous596159751
1172239598172239599AACTCT8GENICheterozygous726375033
1172240054172240055GGCACCCAAA1GENIChomozygous726375034
1172240055172240056GGGCA1GENIChomozygous726375035
1172240448172240449AG11GENICpossibly homozygous596159752
1172240832172240833CT27GENIChomozygous598194623
1172241237172241238CCTT6GENIChomozygous726375036
1172241470172241471GA5GENIChomozygous596159753